CRIS Current Research Information System

CERONI, FABIOLA
 Distribuzione geografica
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Continente #
AS - Asia 1.343
NA - Nord America 1.093
EU - Europa 799
SA - Sud America 69
AF - Africa 55
OC - Oceania 1
Totale 3.360
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Nazione #
US - Stati Uniti d'America 1.070
VN - Vietnam 395
IT - Italia 351
SG - Singapore 333
CN - Cina 294
GB - Regno Unito 84
HK - Hong Kong 82
DE - Germania 81
IN - India 69
SE - Svezia 66
BR - Brasile 50
FR - Francia 39
KR - Corea 39
NL - Olanda 33
IE - Irlanda 28
RU - Federazione Russa 24
JO - Giordania 20
PK - Pakistan 20
CI - Costa d'Avorio 18
BG - Bulgaria 17
FI - Finlandia 17
JP - Giappone 15
BD - Bangladesh 14
TR - Turchia 14
ES - Italia 11
CA - Canada 10
TG - Togo 10
ZA - Sudafrica 10
AT - Austria 9
PH - Filippine 9
AR - Argentina 8
ID - Indonesia 8
UA - Ucraina 7
CH - Svizzera 5
EC - Ecuador 5
IQ - Iraq 5
MA - Marocco 5
MX - Messico 5
TW - Taiwan 5
AE - Emirati Arabi Uniti 4
BE - Belgio 4
EE - Estonia 4
IR - Iran 4
LB - Libano 4
SA - Arabia Saudita 4
SC - Seychelles 4
CZ - Repubblica Ceca 3
DK - Danimarca 3
LT - Lituania 3
PL - Polonia 3
AL - Albania 2
HN - Honduras 2
HR - Croazia 2
NG - Nigeria 2
PY - Paraguay 2
TH - Thailandia 2
AU - Australia 1
BY - Bielorussia 1
CG - Congo 1
CL - Cile 1
CO - Colombia 1
CR - Costa Rica 1
DZ - Algeria 1
EG - Egitto 1
GT - Guatemala 1
JM - Giamaica 1
KZ - Kazakistan 1
LC - Santa Lucia 1
LK - Sri Lanka 1
MD - Moldavia 1
ML - Mali 1
PA - Panama 1
PE - Perù 1
RS - Serbia 1
SN - Senegal 1
SV - El Salvador 1
TN - Tunisia 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 3.360
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Città #
Singapore 231
Ashburn 140
Ho Chi Minh City 100
Bologna 97
Hanoi 89
San Jose 85
Hefei 79
Hong Kong 79
Santa Clara 75
Chandler 72
Southend 67
Fairfield 50
Seoul 37
Redmond 32
Dallas 31
Milan 31
Beijing 28
Dublin 28
Houston 28
Boardman 26
New York 24
Princeton 24
Woodbridge 23
Los Angeles 22
Munich 21
Amman 20
Haiphong 20
Abidjan 18
Council Bluffs 18
Florence 18
Hyderabad 17
Lauterbourg 17
Sofia 17
Seattle 16
Wilmington 16
Ann Arbor 14
Cambridge 13
Bengaluru 12
Rome 12
Tokyo 12
Buffalo 11
Ha Long 11
Helsinki 11
Modena 11
Guangzhou 10
Lomé 10
São Paulo 10
Da Nang 9
Berlin 8
Hải Dương 8
San Diego 8
Des Moines 7
Nanjing 7
Nuremberg 7
Parma 7
Thái Nguyên 7
Amsterdam 6
Biên Hòa 6
Chicago 6
Frankfurt am Main 6
Izmir 6
Jakarta 6
New Delhi 6
Palermo 6
Phoenix 6
Redondo Beach 6
Shekhupura 6
Stockholm 6
Thái Bình 6
Vienna 6
Brooklyn 5
Changsha 5
Chengdu 5
Islamabad 5
Johannesburg 5
Shanghai 5
Turin 5
Turku 5
Xi'an 5
Atlanta 4
Bari 4
Bắc Giang 4
Cesena 4
Dong Ket 4
Dongguan 4
Ferrara 4
Lahore 4
Montreal 4
Padova 4
Quận Bình Thạnh 4
Shenyang 4
Westminster 4
Bern 3
Blacksburg 3
Boydton 3
Brno 3
Brussels 3
Fortaleza 3
Haikou 3
Jeddah 3
Totale 2.106
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Nome #
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder. 354
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates 307
Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility 271
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes 247
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 233
Investigating the role of rare missense variants in RAB11B in Autism Spectrum Disorder 201
Biallelic variants in the small optic lobe calpain CAPN15 are associated with congenital eye anomalies, deafness and other neurodevelopmental deficits 197
Contribution of CACNA1H variants in Autism Spectrum Disorder Susceptibility 186
A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. 153
Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia 141
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. 140
Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia 137
Genome-wide analysis identifies a role for common copy number variants in specific language impairment 124
Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation 115
New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders 109
New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies 109
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies 106
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people 85
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' 85
Discovery of 42 genome-wide significant loci associated with dyslexia 79
null 63
Totale 3.442
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Categoria #
all - tutte 8.888
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 8.888
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202133 0 0 0 0 0 0 0 0 0 0 0 33
2021/2022310 20 4 27 9 39 11 4 20 15 21 94 46
2022/2023325 23 37 16 29 16 42 18 24 66 9 35 10
2023/2024160 13 27 10 19 16 36 3 3 8 5 9 11
2024/2025634 33 77 80 37 107 39 66 10 27 27 54 77
2025/20261.626 228 264 125 153 148 66 123 83 213 102 65 56
Totale 3.442